Hopane-3beta,22-diol
Hopane-3beta,22-diol is a natural product from Iodes cirrhosa.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to
24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
Sci Rep.2024, 14(1):31213.
Toxicol Appl Pharmacol.2022, 434:115815.
Chem Biol Interact.2023, 378:110487.
Earth Environ. Sci. 2021, 905:012080.
Molecules.2018, 23(7):E1659
Appl Microbiol Biotechnol.2024, 108(1):207.
J Appl Biol Chem.2024, 67:33,238-244
Cell Death Discov.2023, 9(1):350.
Food Chem.2017, 221:1135-1144
Huazhong Agricultural University2022, pp34.
Related and Featured Products
Eur J Biochem. 1980 Dec;112(3):541-7.
Non-specific biosynthesis of hopane triterpenes by a cell-free system from Acetobacter pasteurianum.[Pubmed:
7460938]
METHODS AND RESULTS:
The same cell-free system transformed (RS)-2,3-epoxy-2,3-dihydro-[12,13-3H]squalene into labelled 3 alpha-hydroxyhop-22(29)-ene, 3 beta-hydroxyhop-22(29)-ene, hopane-3 alpha,22-diol and Hopane-3beta,22-diol. Their radioactivity was similarly confirmed.
CONCLUSIONS:
This bacterial homogenate is thus capable of cyclizing an unnatural substrate, 2,3-epoxy-squalene, into 3-hydroxyhopanoids normally absent in the bacterium.
